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编码光系统I捕光复合体马铃薯脱辅基蛋白2的Lhca3.St.1基因启动子在转基因马铃薯和烟草植株中的活性。

Activity of the promoter of the Lhca3.St.1 gene, encoding the potato apoprotein 2 of the light-harvesting complex of Photosystem I, in transgenic potato and tobacco plants.

作者信息

Nap J P, van Spanje M, Dirkse W G, Baarda G, Mlynarova L, Loonen A, Grondhuis P, Stiekema W J

机构信息

Department of Molecular Biology, Centre for Plant Breeding and Reproduction Research (CPRO-DLO), Wageningen, Netherlands.

出版信息

Plant Mol Biol. 1993 Nov;23(3):605-12. doi: 10.1007/BF00019307.

DOI:10.1007/BF00019307
PMID:8219093
Abstract

We have isolated cDNA and genomic clones for the potato (Solanum tuberosum) apoprotein 2 of the light harvesting complex of Photosystem I, designated Lhca3.St.1. The protein shows all characteristics of the family of chlorophyll a/b-binding proteins. Potato Lhca3.1 gene expression occurs predominantly in leaves, and is transcriptionally regulated by light. One gene copy is present per haploid genome. The sequence of the 5' upstream region was determined. Most boxes identified in the promoter sequences of genes whose expression is light-regulated recur in the Lhca3.St.1 sequence. Functional analyses of the Lhca3.St.1 promoter and two deletion derivatives in transgenic potato transformed with a promoter-GUS fusion show high promoter activity in leaves and other green parts of the plant, which depends on light. Activity is absent in roots and potato tubers. The 500 bp promoter fragment is as active as the full 2.0 kb sequence, showing that all regulatory elements are present on the smallest deletion derivative. In transgenic tobacco (Nicotiana tabacum) plants carrying the largest promoter derivative a similar distribution of activity is found. Promoter activity is not restricted to the phloem, but also prominent in the xylem of the young stem, which contrasts with promoters of other photosynthesis-associated genes.

摘要

我们已经分离出了马铃薯(Solanum tuberosum)光系统I捕光复合体脱辅基蛋白2的cDNA和基因组克隆,命名为Lhca3.St.1。该蛋白具有叶绿素a/b结合蛋白家族的所有特征。马铃薯Lhca3.1基因主要在叶片中表达,并受光的转录调控。单倍体基因组中存在一个基因拷贝。测定了其5'上游区域的序列。在受光调控基因的启动子序列中鉴定出的大多数元件在Lhca3.St.1序列中重复出现。用启动子-GUS融合转化的转基因马铃薯中,对Lhca3.St.1启动子及其两个缺失衍生物进行功能分析,结果表明该启动子在植物的叶片和其他绿色部分具有高活性,且依赖于光。根和马铃薯块茎中没有活性。500 bp的启动子片段与完整的2.0 kb序列活性相同,表明所有调控元件都存在于最小的缺失衍生物上。在携带最大启动子衍生物的转基因烟草(Nicotiana tabacum)植株中也发现了类似的活性分布。启动子活性不仅限于韧皮部,在幼茎的木质部中也很显著,这与其他光合作用相关基因的启动子不同。

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A study on the influence of different promoter and 5'UTR (URM) cassettes from Arabidopsis thaliana on the expression level of the reporter gene β glucuronidase in tobacco and cotton.关于不同启动子和 5'UTR(URM)盒(阿拉伯idopsis thaliana 的)对报告基因β-葡糖苷酸酶在烟草和棉花中的表达水平的影响的研究。
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